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FDA 510(k)

ATOMLIGHT (LIQUID SCINTILLATION SOLUTION

K-Number: K801245 · 1980-06-20

ApplicantNew England Nuclear
Decision Date1980-06-20
Product CodeJJJ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ATOMLIGHT (LIQUID SCINTILLATION SOLUTION is the device name listed in this FDA 510(k) record. The listed applicant is New England Nuclear. It received FDA 510(k) clearance on 1980-06-20 under 510(k) number K801245. The device is classified under product code JJJ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ATOMLIGHT (LIQUID SCINTILLATION SOLUTION?

ATOMLIGHT (LIQUID SCINTILLATION SOLUTION is a medical device that received FDA 510(k) clearance on 1980-06-20. The listed applicant is New England Nuclear. The 510(k) number is K801245.

When did ATOMLIGHT (LIQUID SCINTILLATION SOLUTION receive FDA 510(k) clearance?

ATOMLIGHT (LIQUID SCINTILLATION SOLUTION received FDA 510(k) clearance on 1980-06-20, under 510(k) number K801245.

Who is the listed applicant for ATOMLIGHT (LIQUID SCINTILLATION SOLUTION?

The FDA 510(k) record lists New England Nuclear as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ATOMLIGHT (LIQUID SCINTILLATION SOLUTION?

The FDA product code for ATOMLIGHT (LIQUID SCINTILLATION SOLUTION is JJJ.

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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